Canonical Allele Identifier: CA1672894312

Gene: ARMT1

Linked Data

• dbSNP Id: rs1781547619

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151468138A>T , CM000668.2:g.151468138A>T	GRCh38
NC_000006.11:g.151789273A>T , CM000668.1:g.151789273A>T	GRCh37
NC_000006.10:g.151830966A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367294.4:c.559-205A>T MANE Select	ENSP00000356263.3:n.559-205A>T
ENST00000367294.3:c.559-205A>T	ENSP00000356263.3:n.559-205A>T
ENST00000494826.1:c.*282-205A>T	ENSP00000435882.1:n.*282-205A>T
ENST00000545879.5:c.202-205A>T	ENSP00000444121.1:n.202-205A>T
NM_001286562.1:c.202-205A>T	NP_001273491.1:n.202-205A>T
NM_024573.2:c.559-205A>T	NP_078849.1:n.559-205A>T
NM_024573.3:c.559-205A>T MANE Select	NP_078849.1:n.559-205A>T
NM_001286562.2:c.202-205A>T	NP_001273491.1:n.202-205A>T